Assurance Infusion recalls TRIMIX (UA) 30MG/1MG/20MCG/ML INJ vials due to lack of sterility assurance. Affected vials have lot number 11042019 and expire 05/02/2020.
Lack of sterility assurance.
Assurance Infusion is recalling TRIMIX (UA) 30MG/1MG/20MCG/ML INJ vials because they lack sterility assurance. This could lead to infections if used improperly. The recall affects vials with lot number 11042019 that expire May 2, 2020.
The vials lack sterility assurance, meaning they may contain harmful bacteria or other contaminants. If used without proper sterilization, this could cause infections in patients. The hazard is specific to the manufacturing process and not a typical use issue.
Healthcare professionals and patients using TRIMIX (UA) 30MG/1MG/20MCG/ML INJ vials with lot number 11042019 are affected. Those who have used the vials without proper sterility checks are at higher risk.
Check for lot number 11042019 on the vial label. The vials expire May 2, 2020. This recall applies to TRIMIX (UA) 30MG/1MG/20MCG/ML INJ in 1 mL vials.
Look for lot number 11042019 on the vial label.
Assurance Infusion is recalling TRIMIX (UA) 30MG/1MG/20MCG/ML INJ vials due to lack of sterility assurance.
Lot number 11042019.
The vials expire May 2, 2020.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0774-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0774-2020 from Assurance Infusion. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
